| Job alert | Jobs 21 - 30 of 110 |
SPD Case Cart Tech
The Nemours Foundation
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Wilmington, DE
... (CBSPD) Association of perioperative Registered Nurses (AORN) The Joint Commission (TJC) U.S Food and Drug Administration (FDA) Center for Disease Control (CDC) Occupational Safety and Health Administration (OSHA) Association for the Advancement of ... - Jun 12
Quality Engineer I
Terumo Medical Corporation
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Elkton, MD, 21922
... Ensure QA, FDA and ISO compliance in all areas of responsibilities. Participate in Product Review Boards. Identify non-conformance trends and develop technical investigation plans. Investigates and analyze customer/internal complaints. Must comply ... - Jun 02
Clinical Research Coordinator
The Nemours Foundation
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Wilmington, DE
... responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS. Participates in continuous process improvement initiatives and implementation of outcomes Prepares for internal and external audits. Prepares corrective action ... - Jun 12
Supervisor, Clinical Engineering Imaging-Biomedical engineering
Nemours Foundation
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Wilmington, DE, 19801
... Experience working under the regulations specific to medical equipment usage and support: The Joint Commission, CMS, OSHA, MDH, NFPA-99, FDA, SMDA. - Jun 18
Manager, Post Market Surveillance
Terumo Medical Corporation
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Elkton, MD, 21922
... Accountable for the Post Market Complaints Engineering Team and managing the product evaluations process in compliance with applicable regulations and standards such as FDA Quality System Regulation, 21 CFR Part 820, ISO 13485:2016, EU Medical ... - May 31
Regulatory and Audit Compliance Specialist
Blood Bank of Delmarva
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Newark, DE
... BBD is FDA licensed, a member of America's Blood Centers, and accredited by AABB. Responsibilities: The Regulatory and Audit Compliance Specialist (“Specialist”) is responsible for developing and maintaining a risk-based quality auditing program for ... - Jun 14
Cloud Engineering Lead
Corteva Agriscience
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Wilmington, DE, 19894
... Ensure personnel and infrastructure are in compliance with external FDA & SOX regulations and any other relevant regional or local regulations (e.g. GDPR). Participate in audits as required. Develop and maintain close partnerships with associated ... - May 28
Quality Associate
Healgen Scientific Limited
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Swedesboro, NJ, 08085
... Ensure that purchased and manufactured material consistently meets design, QA, and manufacturing requirements and meets regulatory compliance with the FDA, ISO, and the IVD Directive. Responsible for handling quality events such as customer ... - Jun 08
Process Engineer
Keystone Industries
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Gibbstown, NJ
... The Process Engineer will be the technical resource providing support to new and existing manufacturing processes with the goal of ensuring safe, high-quality, FDA compliant processes and identifying opportunities for continuous improvement. ... - Jun 11
Product Manager, Upstream Marketing
Keystone Industries
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Gibbstown, NJ
... Desired Skills Experience with ERP, MRP or similar Inventory Management System Experience with ISO - quality assurance / quality control systems Demonstrated knowledge of FDA, cGMP, OSHA, EPA, MDR standards PMP Certification Experience in product ... - Jun 20